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Technical Lead - C, C++, SQL

On-site United States

Job Summary

Role Summary:
Responsible for ensuring software quality and compliance of neurovascular medical devices through rigorous verification, validation, and regulatory adherence.

Key Responsibilities

• Perform software verification & validation (V&V)
• Develop and execute test protocols
• Ensure compliance with IEC 62304, ISO 13485
• Manage defect tracking and root cause analysis
• Support audits and regulatory submissions
• Maintain traceability and design documentation

Skill Requirements

• Software Quality Engineering
• Medical Device Regulations (FDA, EU MDR)
• Risk Management (ISO 14971, FMEA)
• Test Automation & Manual Testing
• Tools: JIRA, Azure DevOps
• Programming: Python/C/C++

Other Requirements

Bachelor’s/Master’s in Engineering (Software, Biomedical, Electronics) with experience in medical device software quality.

software verification & validation (V&V), execute software test protocols.

Source: the employer's careers page. Last checked 2026-10-11. Posted 2026-10-10.

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